Erythrokeratodermia with ataxia | |
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Other names | Giroux–Barbeau syndrome[1] |
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Erythrokeratodermia with ataxia is inherited in an autosomal dominant fashion. | |
Specialty | Medical genetics |
Erythrokeratodermia with ataxia is a condition characterized by erythematous, hyperkeratotic plaques with fine, white, attached scales distributed almost symmetrically on the extremities.[1]